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Prevalence of Plasmodium falciparum Resistance Markers to Sulfadoxine-Pyrimethamine among Pregnant Women Receiving Intermittent Preventive Treatment for Malaria in Uganda

机译:在乌干达接受间歇性疟疾预防治疗的孕妇中,恶性疟原虫耐药标记物对磺胺多辛-乙胺嘧啶的流行性

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The aim of this study was to assess the prevalence of mutations in Plasmodium falciparum dihydrofolate reductase (Pfdhfr) and dihydropteroate synthase (Pfdhps) genes among pregnant women using sulfadoxine-pyrimethamine (SP) as an intermittent preventive treatment (IPTp). A molecular epidemiological study of P. falciparum parasite resistance markers to SP was conducted from August 2010 to February 2012 in Mukono district in central Uganda. DNA was extracted from 413 P. falciparum-positive samples. Real-time PCR, followed by melting curve analysis, was used to characterize point mutations in the Pfdhfr and Pfdhps genes that are associated with SP resistance. The prevalence of the single-nucleotide mutations in Pfdhfr at codons 51I, 59R, and 108N and in Pfdhps at codons 437G and 540E was high (>98%), reaching 100% fixation after one dose of SP, while the prevalence of 581G was 3.3% at baseline, reaching 12.5% after one dose of SP. At baseline, the prevalence of Pfdhfr and Pfdhps quintuple mutations was 89%, whereas the sextuple mutations (including 581G) were not prevalent (3.9%), reaching 16.7% after one dose of SP. However, the numbers of infections at follow-up visits were small, and hence there was insufficient statistical power to test whether there was a true rise in the prevalence of this allele. The overall high frequency of Pfdhfr and Pfdhps quintuple mutations throughout pregnancy excluded further analyses of possible associations between certain haplotypes and the risk of lower birth weight and anemia. However, women infected with P. falciparum had 1.3-g/dl-lower hemoglobin levels (P = 0.001) and delivered babies with a 400-g-lower birth weight (P = 0.001) compared to nonparasitemic women. Despite this, 44 women who were P. falciparum positive at baseline became negative after one or two doses of SP (i.e., 50.5%), implying that SP-IPTp still has some efficacy. P. falciparum resistance markers to SP are high in this population, whereas P. falciparum infection was associated with poor birth outcomes.
机译:这项研究的目的是评估使用磺胺多辛-乙胺嘧啶(SP)作为间歇性预防治疗(IPTp)的孕妇恶性疟原虫二氢叶酸还原酶(Pfdhfr)和二氢蝶呤合酶(Pfdhps)基因突变的普遍性。 2010年8月至2012年2月,在乌干达中部Mukono区进行了恶性疟原虫对SP的抗药性标记的分子流行病学研究。从413个恶性疟原虫阳性样品中提取DNA。实时PCR,然后进行熔解曲线分析,用于鉴定与SP抗性相关的Pfdhfr和Pfdhps基因中的点突变。单核苷酸突变在Pfdhfr的51I,59R和108N密码子和Pfdhps的437G和540E密码子的发生率很高(> 98%),在一剂SP后固定率达到100%,而581G的发生率基线时为3.3%,一剂SP后达到12.5%。在基线时,Pfdhfr和Pfdhps五元组突变的患病率为89%,而六元组突变(包括581G)并不普遍(3.9%),在一剂SP后达到16.7%。但是,随访时的感染数量很少,因此没有足够的统计能力来检验该等位基因的患病率是否确实上升。整个妊娠期间Pfdhfr和Pfdhps五元组突变的总体高频率排除了对某些单倍型与降低出生体重和贫血风险之间可能联系的进一步分析。但是,与非寄生虫妇女相比,感染恶性疟原虫的妇女的血红蛋白水平降低了1.3 g / dl(P = 0.001),分娩的婴儿的出生体重降低了400 g(P = 0.001)。尽管如此,在一到两剂SP(即50.5%)的基础上,基线时恶性疟原虫阳性的44名妇女变为阴性,这表明SP-IPTp仍然有一定疗效。恶性疟原虫对SP的抗性标记在该人群中较高,而恶性疟原虫感染与较差的出生结局有关。

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